Canonical Allele Identifier: CA2581364552
Gene: TBXA2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595406C>A , CM000681.2:g.3595406C>A GRCh38
NC_000019.9:g.3595404C>A , CM000681.1:g.3595404C>A GRCh37
NC_000019.8:g.3546404C>A NCBI36
NG_013363.1:g.16428G>T , LRG_578:g.16428G>T
NG_031943.1:g.14836C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*282G>T MANE Select ENSP00000364336.4:n.*282G>T
ENST00000375190.8:c.*282G>T ENSP00000364336.3:n.*282G>T
ENST00000411851.3:c.984-330G>T ENSP00000393333.2:n.984-330G>T
ENST00000589966.1:c.*145G>T ENSP00000468145.1:n.*145G>T
NM_001060.5:c.*282G>T , LRG_578t1:c.*282G>T NP_001051.1:n.*282G>T
NM_201636.2:c.984-330G>T NP_963998.2:n.984-330G>T
NM_001060.6:c.*282G>T MANE Select NP_001051.1:n.*282G>T
NM_201636.3:c.984-330G>T NP_963998.2:n.984-330G>T